Chia Nan University of Pharmacy & Science Institutional Repository:Item 310902800/24201
English  |  正體中文  |  简体中文  |  全文笔数/总笔数 : 18056/20254 (89%)
造访人次 : 506130      在线人数 : 635
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜寻范围 查询小技巧:
  • 您可在西文检索词汇前后加上"双引号",以获取较精准的检索结果
  • 若欲以作者姓名搜寻,建议至进阶搜寻限定作者字段,可获得较完整数据
  • 进阶搜寻


    jsp.display-item.identifier=請使用永久網址來引用或連結此文件: https://ir.cnu.edu.tw/handle/310902800/24201


    標題: Molecular Design of Bivalent or Dual Action Drugs
    作者: N. S. Zefirov
    V. A.Palyulin
    O. N. Zefirova
    日期: 2011
    上傳時間: 2011-06-23 14:56:57 (UTC+8)
    摘要: Design of new drugs is a sophisticated process involving the application of molecular modeling and QSAR techniques, virtual screening and molecular docking. The joint application of these approaches provides deeper understanding of both structure-activity relationships and ligand-receptor interactions as well as facilitates lead finding and optimization. For the above discussed design the molecular models of all closed and open forms of metabotropic (mGluR1-8) and ionotropic (NMDA andd AMPA) glutamate receptors, adenosine, melatonin, GABAA and GABAc receptors and tubulin have been either built or refined. The docking of known agonists, antagonists, modulators, and channel blockers into the models was used to reveal binding modes of ligands and to explain known structure-activity relationships. Dual action of a drug can be sub-classified into (1) its action on two different biotargets and (2) action on two different sites of the same biotarget. The first case will be exemplified by our design of new neuroprotective compounds. The second will be exemplified by our design of new neuroprotective compounds. The second case will be clarified using (a) the bivalent positive modulator of AMPA receptor and (b) dual action conjugate of colchicine with a "simplified" taxol analogue interacting with tubulin. This approach was successfully used in the design of new neuroprotectors with cognition enhancing properties (extraordinary high potency of some designed compounds starting from picomolar concentration had been revealed - absolute record among all currently known positive AMPA receptor modulators) as well as for synthesis of dual action compounds active against human lung carcinoma A549 cell line.
    關聯: 2011年台俄有機、藥物與生物化學交流暨藥物化學研討會,起迄日:2011/04/06~2011/04/05,地點:溪頭台大實驗林
    显示于类别:[藥理學院] 2011年台俄有機、藥物與生物化學交流暨藥物化學研討會

    文件中的档案:

    档案 描述 大小格式浏览次数
    il-01.pdf101KbAdobe PDF581检视/开启


    在CNU IR中所有的数据项都受到原著作权保护.

    TAIR相关文章

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回馈